Home NDC 79506-100-04 DETROX
Product NDC 79506-100
Requested package NDC 79506-100-04
11-digit product format 795060100
Labeler code 79506
Product ID 79506-100_22399241-cbbd-4248-b8ba-628fe4101534
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler DETRO HEALTHCARE KIMYA SANAYI ANONIM SIRKETI
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-06-30
Marketing end 0000-00-00
Substance ISOPROPYL ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79506-100-01 DETROX- DETRODERM HAND AND SKIN ANTISEPTIC 100 mL in 1 BOTTLE LIQUID 100 1 79506-100-02 DETROX- DETRODERM HAND AND SKIN ANTISEPTIC 250 mL in 1 BOTTLE LIQUID 250 1 79506-100-03 DETROX- DETRODERM HAND AND SKIN ANTISEPTIC 500 mL in 1 BOTTLE LIQUID 500 1 79506-100-04 DETROX- DETRODERM HAND AND SKIN ANTISEPTIC 1000 mL in 1 BOTTLE LIQUID 1000 1 79506-100-05 DETROX- DETRODERM HAND AND SKIN ANTISEPTIC 5000 mL in 1 CAN LIQUID 5000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79506-100 DETROX - DETRODERM HAND AND SKIN ANTISEPTIC (ISOPROPYL ALCOHOL) LIQUID [DETRO HEALTHCARE KIMYA SANAYI ANONIM SIRKETI] 1 Legacy NDC, 5 package rows 20200729_6c32c72e-efd2-4a99-a279-0f3296b06bea.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 79506-100-04 79506010004 1000 mL in 1 BOTTLE (79506-100-04) 1000 ml 2020-06-30 0000-00-00 No No Current